Canonical Allele Identifier: CA2043754604
Gene: IFNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158714_68158730delinsAGTGTGTGTGTGTGTGT , CM000674.2:g.68158714_68158730delinsAGTGTGTGTGTGTGTGT GRCh38
NC_000012.11:g.68552494_68552510delinsAGTGTGTGTGTGTGTGT , CM000674.1:g.68552494_68552510delinsAGTGTGTGTGTGTGTGT GRCh37
NC_000012.10:g.66838761_66838777delinsAGTGTGTGTGTGTGTGT NCBI36
NG_015840.1:g.6012_6028delinsACACACACACACACACT

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-471_115-455delinsACACACACACACACACT MANE Select ENSP00000229135.3:n.115-471_115-455delinsACACACACACACACACT
ENST00000229135.3:c.115-471_115-455delinsACACACACACACACACT ENSP00000229135.3:n.115-471_115-455delinsACACACACACACACACT
NM_000619.2:c.115-471_115-455delinsACACACACACACACACT NP_000610.2:n.115-471_115-455delinsACACACACACACACACT
NM_000619.3:c.115-471_115-455delinsACACACACACACACACT MANE Select NP_000610.2:n.115-471_115-455delinsACACACACACACACACT
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